Influence of Dental Occlusion on the Performance of High Level Rowers (IODPR)

NCT ID: NCT03648125

Last Updated: 2018-08-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

7 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-27

Study Completion Date

2017-11-22

Brief Summary

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Monocentric, prospective, randomized, open-label, cross-over study.

Detailed Description

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Current literature data suggest that dental occlusion has an influence on postural control in the general population, and more markedly in high-level athletes. The link between dental occlusion and the postural stability of top athletes has been studied in several disciplines such as basketball, shooting, golf and running. There is currently no data in the field of rowing. But this sport requires optimal postural control for synchronous and symmetrical muscle solicitation.

The present study aims to evaluate the influence of dental occlusion on postural stability and the performance of high level rowers.

Our assumptions are as follows:

* Occlusal disturbance alters the muscular power developed by high level rowers
* occlusal disturbance alters the static postural stability of high level rowers

Conditions

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Dental Occlusion, Traumatic

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

Prospective, monocentric, randomized, open-label, cross-over study. Randomization applies on the order of the training sessions "with" or "without" occlusal disturbance.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Rowing training session

Power tests, balance and tonicity tests are performed eyes opened and eyes closed :

* with artificial occlusal disturbance and
* without artificial occlusal disturbance

Group Type OTHER

with artificial occlusal disturbance

Intervention Type DEVICE

A silicon artificial occlusal disturbance is made from a mould of the rowers mouth and placed in the mouth during the training session.

With artificial occlusal disturbance : Maximal Intercuspal Occlusion (MIO) with silicone splint increases the vertical dimension of occlusion of 1, 2 and 4 mm.

without artificial occlusal disturbance

Intervention Type DEVICE

The training session is performed without occlusal disturbance

Interventions

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with artificial occlusal disturbance

A silicon artificial occlusal disturbance is made from a mould of the rowers mouth and placed in the mouth during the training session.

With artificial occlusal disturbance : Maximal Intercuspal Occlusion (MIO) with silicone splint increases the vertical dimension of occlusion of 1, 2 and 4 mm.

Intervention Type DEVICE

without artificial occlusal disturbance

The training session is performed without occlusal disturbance

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* High level rower, part of the Lille Rowing Hope Pole;
* At least 15 years old;
* Training at the Centre de Ressources, d'Expertise et de Performance Sportive (CREPS) de Wattignies during the period from 01/09/2017 to 31/10/2017;
* Having at least 28 natural or prosthetic teeth in occlusion;
* Not having consumed alcohol in the last 24 hours before the recordings;
* whose parents have given free, informed and written consent for minors;
* Having given free and informed consent, in writing supplemented by the consent of at least one holder of parental authority, if he is a minor;
* Affiliated, himself or through his parents if he is a minor, to a social security scheme.

Exclusion Criteria

* Current antecedent(s) or pathology(s) likely to disturb the balance: neurological, ear nose and throat, ophthalmological, orthopedic;
* Temporomandibular joint disorder (s) (pain and / or noise);
* Orofacial symptoms (headache, tinnitus, facial myalgia, bruxism);
* Dental and / or periodontal care in progress;
* Chronic pain requiring daily use of analgesics for more than three months;
* Pregnant or lactating woman;
* Concurrent participation in another study;
* Major persons subject to legal protection (safeguard of justice, guardianship, tutorship) and persons deprived of their liberty.
Minimum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Rennes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Xavier MD RAVALEC

Role: PRINCIPAL_INVESTIGATOR

Rennes University Hospital

Locations

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CREPS de Wattignies

Wattignies, Hauts-de-France, France

Site Status

Countries

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France

Other Identifiers

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35RC17_8823_IODPR

Identifier Type: -

Identifier Source: org_study_id

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